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Fig. 5 in Flight patterns and sex ratio of beetles of the subfamily Dynastinae (Coleoptera, Melolonthidae)
Fig. 5. Spearman correlation between sex ratio and rainfall of: (A) Cyclocephala distincta; (B) C. paraguayensis; (C) Tomarus ebenus; (D) L. (Ligyrus) cuniculus.
Figure 2 in Trapping Sweetpotato Weevil, Cylas formicarius (Coleoptera: Brentidae), with High Doses of Sex Pheromone: Catch Enhancement and Weathering Rate in Hawaii
Figure 2. Effect of lure loading on trap catch over one week of weathering. Average (± SEM) male sweetpotato weevil catch per trap per week in sweetpotato fields in the vicinity of Pepeekeo, Hawaii, in traps baited with one of three different loadings of male sweetpotato weevil attractant. Catch results are from the first week following initial trap deployment with five traps for each loading, deployed in a randomized complete block design (average of three separate trials). Bars labeled with the same letter are not significantly different at the α = 0.05 level.
Figure 1 in Trapping Sweetpotato Weevil, Cylas formicarius (Coleoptera: Brentidae), with High Doses of Sex Pheromone: Catch Enhancement and Weathering Rate in Hawaii
Figure 1. Map of weathering trial showing locations of fields where traps with lures were placed (developed using ArcGIS [ESRI 2012]). Traps were initially deployed at Site 1 on 14 February, 2012, and moved on to Sites 2, 3, 4, and 5 over the course of the weathering trial. The weathering time of the traps at each site was as follows: (Site 1) first 8 weeks; (Site 2) weeks 9–16; (Site 3) weeks 17–24; (Site 4) weeks 25–40; and (Site 5) week 41 (assessment). A weather station was maintained over the course of the weathering trial and was located at Site 2 for the first 16 weeks and then located at the location of the filled circle on the map for the remaining weeks of the trial.
Figure 4. Trial 4 in Trapping Sweetpotato Weevil, Cylas formicarius (Coleoptera: Brentidae), with High Doses of Sex Pheromone: Catch Enhancement and Weathering Rate in Hawaii
Figure 4. Trial 4 results: Effect of weathering over 40 weeks on trap catch. Decline in sweetpotato weevil catch/trap/week over 40 weeks in traps baited with (A) septum holding 1.0 mg male lure (see text for calculated exponential decay curve), and (B) septum holding 120 μg male lure (see text for calculated exponential decay curve). Calculated septum age where catch is 50% of fresh catch is presented for each curve.
Fig. 1 in Helminths in common eiders (Somateria mollissima): Sex, age, and migration have differential effects on parasite loads
Fig. 1. Distributions of breeding and wintering populations of S. m. borealis, S. m. dresseri, and S. m. sedentaria in North America and Greenland. Populations of S. m. borealis are wintering in two areas in the pictured region; one in Southwest Greenland and one in East Canada (Newfoundland and Labrador). Individuals wintering in Southwest Greenland migrate to breed in West Greenland or Arctic Canada, whereas individuals wintering in East Canada have breeding areas in Arctic Canada (illustrated by the different direction of the red diagonal lines). For S. m. dresseri the breeding and wintering ranges overlap in one area that covers Newfoundland and Labrador as well as the northeastern part of the US, as shown by the grey horizontal lines. The subspecies S. m. sedentaria has its year-round residence in the Hudson Bay area as shown by the blue vertical lines. Dark stars mark the sampling locations of eiders in this study, whereas the white star marks the sampling location of eiders by Tourangeau et al. (2018). (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
Fig. 3 in Helminths in common eiders (Somateria mollissima): Sex, age, and migration have differential effects on parasite loads
Fig. 3. Prevalences of the cestodes Lateriporus sp. (A) and Microsomacanthus spp. (B), and the acanthocephalan Profilicollis sp. (C) in common eiders. Abbreviations: bor, CD = S. m. borealis, Cape Dorset; bor, GRLD = S. m. borealis, Greenland; bor, NFLD = S. m. borealis, Newfoundland; dre, NFLD = S. m. dresseri, Newfoundland; sed, BI = S. m. sedentaria [data published in Tourangeau et al. (2018)]. n-m = non-migratory, po-m = post-migratory, prm = pre-migratory. Letters describe significant differences between groups: if two groups share a letter, there is no significant difference in their prevalences.
Fig. 2 in Helminths in common eiders (Somateria mollissima): Sex, age, and migration have differential effects on parasite loads
Fig. 2. Examples of gastrointestinal parasites retrieved from common eiders in this study. (A) The trematode Notocotylus sp., (B) the cestode Lateriporus sp., (C) the acanthocephalan, Profilicollis sp. (D) microphallid trematodes, and (E) Microsomacanthus spp. cestodes.
Fig. 5 in Helminths in common eiders (Somateria mollissima): Sex, age, and migration have differential effects on parasite loads
Fig. 5. Cumulative percentages of birds infected with (A) Microsomacanthus spp., (B) Microphallus spp. and (C) Gymnophallus spp. from five different locations. Legend denotes the five infection levels: 0, 1s, 10s, 100s, and 1000s of parasite individuals within a single host. Abbreviations: bor, GRLD = S. m. borealis, Greenland; bor, NFLD = S. m. borealis, Newfoundland; dre, NFLD = S. m. dresseri, Newfoundland; bor, CD = S. m. borealis, Cape Dorset; sed, BI = S. m. sedentaria, Belcher Islands [data published in (Tourangeau et al., 2018)]. nm = non-migratory, po-m = post-migratory, pr-m = pre-migratory.
Figure 5 in Diurnal activity pattern of age-sex groups of a small and fragmented population of Blackbuck (Antilope cervicapra L.) in Western Haryana, India
Figure 5. Behavioural activities recorded for sub adult male vs. total time spent during different season(s).
Figure 6 in Diurnal activity pattern of age-sex groups of a small and fragmented population of Blackbuck (Antilope cervicapra L.) in Western Haryana, India
Figure 6. Behavioural activities recorded for sub adult female vs. total time spent during different season(s).
Figure 3 in Diurnal activity pattern of age-sex groups of a small and fragmented population of Blackbuck (Antilope cervicapra L.) in Western Haryana, India
Figure 3. Behavioural activities recorded for adult male vs. total time spent during different season(s).
Figure 4 in Diurnal activity pattern of age-sex groups of a small and fragmented population of Blackbuck (Antilope cervicapra L.) in Western Haryana, India
Figure 4. Behavioural activities recorded for adult female vs. total time spent during different season(s).
Figure 8 in Diurnal activity pattern of age-sex groups of a small and fragmented population of Blackbuck (Antilope cervicapra L.) in Western Haryana, India
Figure 8. Average % time spent annually versus activities by different age sex group (Error bars with standard error and treatment bars with different letters differ significantly at P ≤ 0.05 based on Duncan Multiple Range Test).
Figure 7 in Diurnal activity pattern of age-sex groups of a small and fragmented population of Blackbuck (Antilope cervicapra L.) in Western Haryana, India
Figure 7. Major behavioural activities vs. total time spent on each activity by different age-sex animal.
Text-fig. 9. Sex estimation of Moča skull (Komárno district, southern Slovakia), linear discriminant analysis using Henke's Late Upper Palaeolithic and Mesolithic database (n = 129, f = 46, m = 83), as well as according to recent Howells's database (n = 2524, f = 1156, m = 1368) with variables M1 (GOL) and M45 (ZYB). in A Late Upper Palaeolithic Skull From Moča (The Slovak Republic) In The Context Of Central Europe
Text-fig. 9. Sex estimation of Moča skull (Komárno district, southern Slovakia), linear discriminant analysis using Henke's Late Upper Palaeolithic and Mesolithic database (n = 129, f = 46, m = 83), as well as according to recent Howells's database (n = 2524, f = 1156, m = 1368) with variables M1 (GOL) and M45 (ZYB).
Figure 3 in Sex ratio estimations of Chelonia mydas hatchlings at Samandağ Beach, Turkey
Figure 3. The maximum increase and decrease in two nests' temperatures throughout the incubation duration.
Figure 5 in Reproductive pattern and sex hormones of Calotes emma Gray 1845 and Calotes versicolor Daudin 1802 (Squamata; Agamidae)
Figure 5. Photomicrographs of annual changes in C. versicolor. Top left, testes; top right, male SSK; bottom left, ovaries; bottom right, granulosa layers (GL). Notes: SZ, spermatozoa; ST, seminiferous tubules; SSK, sexual segments of kidney; AF, atretic follicle; PF, previtellogenic follicle; VF, vitellogenic follicle; P, pyriform cells; S, small cells; CL, corpus luteum.
Figure 6 in Reproductive pattern and sex hormones of Calotes emma Gray 1845 and Calotes versicolor Daudin 1802 (Squamata; Agamidae)
Figure 6. Annual profiles (mean ± SEM) of testosterone levels and testicular masses (a) C. emma; (b) C. versicolor. Notes: Jan– Dec denotes January to December. The numbers (in parentheses) represent the number of analyzed samples in each month.
Figure 3 in Reproductive pattern and sex hormones of Calotes emma Gray 1845 and Calotes versicolor Daudin 1802 (Squamata; Agamidae)
Figure 3. Schematics of seasonal changes in ovarian size. Top, C. emma; bottom, C. versicolor. Notes: OvaF, ovarian follicles; OviE, oviductal eggs; Ovi, oviduct. All scale bars equals 5 mm. Jan–Nov denotes from January to November.
Figure 2 in Reproductive pattern and sex hormones of Calotes emma Gray 1845 and Calotes versicolor Daudin 1802 (Squamata; Agamidae)
Figure 2. Schematics of annual changes in testicular size. Top; C. emma; bottom, C. versicolor. Notes: T, testis; Vd, vas deferens; K, kidney. Jan–Dec denotes from January to December. All scale bars equal 5 mm.
ScienceDex guides
Understand access before you commit
These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.